WO2001090109A1 - Heteroaryldiazabicycloalkanes comme ligands du recepteur cholinergique nicotinique - Google Patents

Heteroaryldiazabicycloalkanes comme ligands du recepteur cholinergique nicotinique Download PDF

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WO2001090109A1
WO2001090109A1 PCT/US2001/016941 US0116941W WO0190109A1 WO 2001090109 A1 WO2001090109 A1 WO 2001090109A1 US 0116941 W US0116941 W US 0116941W WO 0190109 A1 WO0190109 A1 WO 0190109A1
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substituted
nitrogen
substituent species
hydrogen
diazabicyclo
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PCT/US2001/016941
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WO2001090109A9 (fr
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Craig Harrison Miller
Gary Maurice Dull
Lan Miao
Dwo Lynm
Jeffrey Daniel Schmitt
Thomas Jeffrey Clark
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Targacept, Inc.
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Priority claimed from US09/578,768 external-priority patent/US6440970B1/en
Priority to EP01941614A priority Critical patent/EP1289996B1/fr
Priority to AU2001274952A priority patent/AU2001274952A1/en
Priority to BR0110956-1A priority patent/BR0110956A/pt
Priority to DK01941614T priority patent/DK1289996T3/da
Priority to AT01941614T priority patent/ATE292636T1/de
Application filed by Targacept, Inc. filed Critical Targacept, Inc.
Priority to JP2001586296A priority patent/JP2003534344A/ja
Priority to CA002409644A priority patent/CA2409644A1/fr
Priority to MXPA02011261A priority patent/MXPA02011261A/es
Priority to DE60109924T priority patent/DE60109924T2/de
Publication of WO2001090109A1 publication Critical patent/WO2001090109A1/fr
Publication of WO2001090109A9 publication Critical patent/WO2001090109A9/fr

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/08Bridged systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/26Psychostimulants, e.g. nicotine, cocaine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Definitions

  • the present invention relates to pharmaceutical compositions, particularly pharmaceutical compositions incorporating compounds that are capable of affecting nicotinic cholinergic receptors. More particularly, the present invention relates to compounds capable of activating nicotinic cholinergic receptors, for example, as agonists of specific nicotinic receptor subtypes. The present invention also relates to methods for treating a wide variety of conditions and disorders, particularly conditions and disorders associated with dysfunction of the central and autonomic nervous systems.
  • Nicotine has been proposed to have a number of pharmacological effects. See, for example, Pullan et al., N. Engl. J. Med. 330:811 (1994). Certain of those effects may be related to effects upon neurotransmitter release. See, for example, Sjak-shie et al., Brain Res. 624:295 (1993), where neuroprotective effects of nicotine are proposed. Release of acetylcholine and dopamine by neurons upon administration of nicotine has been reported by Rowell et al., J Neurochem. 43:1593 (1984); Rapier et al, J Neurochem. 50:1123 (1988); Sandor et al., Brain Res. 567:313 (1991) and Nizi, Br. J. Pharmacol.
  • Nicotinic compounds are reported as being particularly useful for treating a wide variety of CNS disorders. Indeed, a wide variety of compounds have been reported to have therapeutic properties. See, for example, U.S. Patent Nos. 5,1871,166 to Kikuchi et al., 5,672,601 to Cignarella, PCT WO 99/21834 and PCT WO 97/40049, UK Patent Application GB 2295387 and European Patent Application 297,858.
  • CNS disorders are a type of neurological disorder.
  • CNS disorders can be drug induced; can be attributed to genetic predisposition, infection or trauma; or can be of unknown etiology.
  • CNS disorders comprise neuropsychiatric disorders, neurological diseases and mental illnesses, and include neurodegenerative diseases, behavioral disorders, cognitive disorders and cognitive affective disorders.
  • CNS disorders whose clinical manifestations have been attributed to CNS dysfunction (i.e., disorders resulting from inappropriate levels of neurotransmitter release, inappropriate properties of neurotransmitter receptors, and/or inappropriate interaction between neurotransmitters and neurotransmitter receptors).
  • CNS disorders can be attributed to a deficiency of choline, dopamine, norepinephrine and/or serotonin.
  • Relatively common CNS disorders include pre-senile dementia (early- onset Alzheimer's disease), senile dementia (dementia of the Alzheimer's type), micro-infarct dementia, AIDS-related dementia, Creutzfeld- Jakob disease, Pick's disease, Parkinsonism including Parkinson's disease, progressive supranuclear palsy, Huntington's chorea, tardive dyskinesia, hyperkinesia, mania, attention deficit disorder, anxiety, dyslexia, schizophrenia, depression, obsessive-compulsive disorders and Tourette's syndrome.
  • CNS diseases e.g., CNS diseases
  • the present invention relates to diazabicyclic compounds, and preferably N- aryl diazabicyclic compounds. Of particular interest are certain substituted N-pyridyl diazabicyclic compounds.
  • Exemplary compounds of the present invention include: (1 S,4S)-2-(5-(3-methoxyphenoxy)-3-pyridyl)-2,5-diazabicyclo[2.2.1 Jheptane, (lS,4S)-2-(5-(4-methoxyphenoxy)-3-pyridyl)-2,5-diazabicyclo[2.2.1]heptane, (1 S,4S)-2-(5-(4-fluorophenoxy)-3-pyridyl)-2,5-diazabicyclo[2.2.
  • the present invention also relates to methods for the prevention or treatment of a wide variety of conditions or disorders, particularly those disorders characterized by dysfunction of nicotinic cholinergic neurotransmission including disorders involving neuromodulation of neurotransmitter release, such as dopamine release.
  • the present invention also relates to methods for the prevention or treatment of disorders, such as central nervous system (CNS) disorders, which are characterized by an alteration in normal neurotransmitter release.
  • CNS central nervous system
  • the present invention also relates to methods for the treatment of certain conditions (e.g., a method for allevr ⁇ ting pain). The methods involve administering to a subject an effective amount of a compound of the present invention.
  • the present invention in another aspect, relates to a pharmaceutical composition
  • a pharmaceutical composition comprising an effective amount of a compound of the present invention.
  • a pharmaceutical composition incorporates a compound which, when employed in effective amounts, has the capability of interacting with relevant nicotinic receptor sites of a subject, and hence has the capability of acting as a therapeutic agent in the prevention or treatment of a wide variety of conditions and disorders, particularly those disorders characterized by an alteration in normal neurotransmitter release.
  • Preferred pharmaceutical compositions comprise compounds of the present invention.
  • compositions of the present invention are useful for the prevention and treatment of disorders, such as CNS disorders, which are characterized by an alteration of normal neurotransmitter release.
  • the pharmaceutical compositions provide therapeutic benefit to individuals suffering from such disorders and exhibiting clinical manifestations of such disorders in that the compounds within those compositions, when employed in effective amounts, have the potential to: (i) exhibit nicotinic pharmacology and affect relevant nicotinic receptors sites (e.g., act as a pharmacological agonist to activate nicotinic receptors), and/or (ii) modulate neurotransmitter secretion and thus prevent and suppress the symptoms associated with those diseases.
  • the compounds are expected to have the potential to fulfill the following results for the patient: (i) to alter the number of nicotinic cholinergic receptors of the brain of the patient, (ii) to exhibit neuroprotective effects and (iii) to result in no appreciable adverse side effects when administered in effective amounts— side effects such as significant increases in blood pressure and heart rate, significant negative effects upon the gastro-intestinal tract, and significant effects upon skeletal muscle.
  • the pharmaceutical compositions of the present invention are believed to be safe and effective with regards to prevention and treatment of a wide variety of conditions and disorders.
  • the compounds of the present invention include compounds having a diazabicyclic ring.
  • the structure can be represented by the formula:
  • Q is (CH 2 ) U
  • Q j is (CH 2 ) V
  • Q H is (CH 2 ) W
  • Q ni is (CH 2 ) X
  • Q iv is (CH 2 ) y
  • R is hydrogen or lower alkyl, preferably hydrogen.
  • the values of u, v, w, x and y are selected such that the resulting diazabicyclic ring contains 7, 8 or 9 members, preferably 7 members.
  • Z represents a suitable non-hydrogen substituent species; exemplary species are set forth hereinafter.
  • j is an integer from 0 to 10, preferably 0, 1 or 2.
  • Cy represents a suitably substituted 6-membered aromatic ring, as represented by the formula:
  • each of X, X' and X" are individually nitrogen, nitrogen bonded to oxygen (e.g., an N-oxide or other N-O functionality) or carbon bonded to a substituent species (i.e., hydrogen or a non-hydrogen species);
  • D is a suitable non-hydrogen substituent species, as set forth hereinafter;
  • k is either 0, 1 or 2, preferably 0 or 1 ; and
  • Cx is selected from a group consisting of aryl, substituted aryl, heteroaryl, substituted heteroaryl, non-aromatic heterocyclyl, substituted non- aromatic heterocyclyl, non-aromatic heterocyclylalkyl and substituted non-aromatic heterocyclylalkyl.
  • A can also be a covalent bond, with the proviso that when A is so defined, the diazabicyclic ring is not 2,5-diazabicyclo[2.2.1]heptane and/or Cx is not phenyl or substituted phenyl.
  • Cx is aryl or heteroaryl.
  • R 1 and R" can form a cycloalkyl functionality.
  • Representative aromatic groups include carbocyclic (phenyl, biphenyl, naphthyl, etc.) and heterocyclic (pyridinyl, pyrimidinyl, quinolinyl, indolyl, etc.) rings.
  • alkyl refers to straight chain or branched alkyl radicals including -Cg, preferably Ci-Cs, such as methyl, ethyl, or isopropyl, and cyclic alkyl radicals up to 8 carbons; "substituted alkyl” refers to alkyl radicals further bearing one or more substituent species such as hydroxy, alkoxy, mercapto, aryl, heterocyclo, halo, amino, carboxyl, carbamyl, cyano, and the like; "alkenyl” refers to straight chain or branched hydrocarbon radicals including Ci-C 8 , preferably -Cs and having at least one carbon-carbon double bond; “substituted alkenyl” refers to alkenyl radicals further bearing one or more substituent species as defined above; "aryl” refers to aromatic radicals having six to ten carbon atoms; “substituted aryl” refers to aryl radicals further
  • heteroaryl refers to heterocyclic aromatic radicals, such as pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, quinolinyl, furanyl, thienyl, pyrrolyl, indolyl, benzoxazolyl, etc.
  • non-aromatic heterocyclyl refers to heterocyclic radicals, saturated or unsaturated, which are not aromatic, such as tetrahydrofuranyl, tetrahydropyranyl, tetrahydrothienyl, tetrahydrothiopyranyl, pyrrolidinyl, piperidinyl, etc.
  • non-aromatic heterocyclylalkyl refers to non- aromatic heterocyclyl radicals attached through an alkylene chain of up to four carbon atoms; in each case, “substituted” refers to the replacement of one or more of the hydrogens
  • the preferred embodiments of the invention are those in which one or two of X, X' and X" are nitrogen, the most preferred being the case in which only X" is nitrogen.
  • X is nitrogen
  • A is attached at the C-5 position of the pyridine ring and that k is 0 or 1.
  • Cx is preferably:
  • Y, Y', Y" and Y"' are individually nitrogen, nitrogen bonded to oxygen, or carbon bonded to hydrogen or a substituent species, G;
  • E is oxygen, sulfur or nitrogen bonded to hydrogen or a substituent species, G;
  • E', E" and E'" are individually nitrogen or carbon bonded to hydrogen or a substituent species, G;
  • m is 0, 1, 2, 3 or 4;
  • p is 0, 1, 2 or 3;
  • n is 0, 1, 2, 3 or 4;
  • G is selected from the group consisting of alkyl, substituted alkyl, alkenyl, substituted alkenyl, non-aromatic heterocyclyl, substituted non-aromatic heterocyclyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkylaryl, substituted alkylaryl, arylalkyl, substituted arylalkyl, substituted arylalkyl, -F, -CI, -Br, -I
  • Y, Y', Y", Y'", E', E” and E'" are all carbon bonded to a substituent species.
  • one or two of Y, Y', Y", Y'", E', E” and E'" are nitrogen and the remaining are carbon bonded to a substituent species.
  • R' and R" can form a cycloalkyl functionality.
  • Representative aromatic groups include carbocyclic (phenyl, biphenyl, naphthyl, etc.) and heterocyclic (pyridinyl, pyrimidinyl, quinolinyl, indolyl, etc. ) rings.
  • Adjacent non-hydrogen substituent species, G may combine to form one or more saturated or unsaturated, substituted or unsubstituted, carbocyclic or heterocyclic rings containing, but not limited to, ether, acetal, ketal, amine, ketone, lactone, lactam, carbamate and urea functionalities.
  • Representative compounds of the present invention include the following: (lS,4S)-2-(5-phenoxy-3-pyridyl)-2,5-diazabicyclo[2.2.1]heptane (lR,4R)-2-(5-phenoxy-3-pyridyl)-2,5-diazabicyclo[2.2.1]heptane ( 1 S,4S)-2-(5-(3 -methoxyphenoxy)-3 -pyridyl)-2,5-diazabicyclo [2.2.1 ]heptane (lR,4R)-2-(5-(3-methoxyphenoxy)-3-pyridyl)-2,5-diazabicyclo[2.2.1]heptane (lS,4S)-2-(5-(4-methoxyphenoxy)-3-pyridyl)-2,5-diazabicyclo[2.2.1]heptane (lS,4S)-2-(5-(4-methoxyphenoxy
  • the following compounds also are representative compounds of the present invention: 6-methyl-3 -(5 -phenyl-3 -pyridyl)-3 ,6-diazabicyclo [3.2.1 joctane 6-methy 1-3 -(5 -phenoxy-3 -pyridyl)-3 ,6-diazabicyclo [3.2.1] octane 6-methyl-3 -(5-(3 -methoxyphenoxy)-3 -pyridyl)-3 ,6-diazabicyclo [3.2.1 ]octane 6-methyl-3-(5-(4-methoxyphenoxy)-3-pyridyl)-3,6-diazabicyclo[3.2.1]octane 6-methyl-3 -(5-(3 ,4-dimethoxyphenoxy)-3 -pyridyl)-3 ,6-diazabicyclo [3.2.1 ]octane 6-methyl-3-(5-(3 ,4-dimethoxy
  • N-aryl diazabicyclic compounds of the present invention are synthetically produced can vary.
  • Commercially available (Aldrich Chemical) (lS,4S)-N-(tert-butoxycarbonyl)-2,5-diazabicyclo[2.2.1]heptane can be coupled with a variety of aromatic halides and heteroaromatic halides using palladium catalysis. See Yang et al., J Organomet. Chem. 576: 125 (1999), Wolfe et al., Ace. Chem. Res. 31:805 (1998) and Hartwig et al., J Org. Chem. 64: 5575 (1999).
  • the N-tert- butoxycarbonyl protecting group is readily removed in the presence of acid to provide (lS,4S)-2-(5-bromo-3-pyridyl)-2,5-diazabicyclo[2.2.1]heptane.
  • Use of the other enantiomer, (lR,4R)-N-(tert-butoxycarbonyl)-2,5-diazabicyclo[2.2.1]heptane, in the palladium-catalyzed coupling will lead to (lR,4R)-2-(5-bromo-3-pyridyl)-2,5- diazabicyclo[2.2.1]heptane.
  • Both the (1S,4S) and the (1R,4R) enantiomers of the N- (tert-butoxycarbonyl)-2,5-diazabicyclo[2.2.1]heptane can be synthesized from hydroxyproline isomers as described in US Patent Nos. 5,095,121 and 5,196,548 to Braish and Fox and by Braish and Fox in J. Org. Chem. 55:1694 (1990). Also reported in these references are the syntheses of the N-benzyl derivatives of (1S,4S)- and (lR,4R)-2,5-diazabicyclo[2.2.1]heptane.
  • a suitably protected derivative of either 2-(5-bromo-3-pyridyl)-2,5- diazabicyclo[2.2.1]heptane enantiomer can be elaborated to give a number of compounds possessing substituents at the C-5 position of the pyridine.
  • 5-benzyl-2-(5-bromo-3-pyridyl)-2,5-diazabicyclo[2.2.1]heptane can be converted into the corresponding 5-amino-substituted compound by the general method of Zwart et al., Recueil Trav. Chim.
  • 5- Alkylamino-substituted compounds can be prepared in a similar manner.
  • 5-Ethynyl- substituted compounds can be prepared from the 5-bromo-substituted compound by palladium-catalyzed coupling using 2-methyl-3-butyn-2-ol, followed by base- catalyzed (sodium hydride) removal of the acetone unit, according to the general techniques described in Cosford et al., J. Med. Chem. 39:3235 (1996).
  • the 5-ethynyl analogs can be converted into the corresponding 5-ethenyl and subsequently to the corresponding 5-ethyl analogs by successive catalytic hydrogenation reactions (which would also remove the benzyl protecting group from the diazabicycle).
  • the 5-azido- substituted analogs can be prepared from the 5-bromo-substituted compound by reaction with lithium azide in N,N-dimethylformamide.
  • 5-Alkylthio-substituted analogs can be prepared from the 5-bromo-substituted compound by reaction with an appropriate sodium alkylmercaptide (sodium alkanethiolate), using techniques known to those skilled in the art of organic synthesis.
  • a number of other analogs, bearing substituents in the 5 position of the pyridine ring, can be synthesized from 5-benzyl-2-(5-amino-3-pyridyl)-2,5- diazabicyclo[2.2.1]heptane (the synthesis of which is described above) via the 5- diazonium salt intermediate. Either enantiomer of the 5-amino compound may be utilized.
  • 5-substituted analogs that can be produced from 5- diazonium salt intermediates are: 5-hydroxy analogs, 5-alkoxy analogs, 5-fluoro analogs, 5-chloro analogs, 5-bromo analogs, 5-iodo analogs, 5-cyano analogs, and 5- mercapto analogs.
  • 5-hydroxy-substituted analogs can be prepared from the reaction of the corresponding 5-diazonium salt intermediates with water.
  • 5-Alkoxy analogs can be made from the reaction of the diazonium salts with alcohols.
  • 5-Fluoro-substituted analogs can be prepared from the reaction of the 5- diazonium salt intermediates with fluoroboric acid.
  • 5-Chloro-substituted analogs can be prepared from the reaction of the 5-amino compounds with sodium nitrite and hydrochloric acid in the presence of copper chloride.
  • 5-Cyano-substituted analogs can be prepared from the reaction of the corresponding 5-diazonium salt intermediates with potassium copper cyanide.
  • Appropriate 5-diazonium salt intermediates can also be used for the synthesis of mercapto-substituted analogs using the general techniques described in Hoffman et al., J Med. Chem. 36:953 (1993).
  • the 5-mercapto- substituted analogs can in turn be converted to the 5-alkylthio-substituted analogs by reaction with sodium hydride and an appropriate alkyl bromide.
  • 5-Acylamido analogs of the aforementioned compounds can be prepared by reaction of the corresponding 5- amino compounds with an appropriate acid anhydride or acid chloride using techniques known to those skilled in the art of organic synthesis.
  • 5-Hydroxy-substituted analogs of the aforementioned compounds can be used to prepare corresponding 5-alkanoyloxy-substituted compounds by reaction with the appropriate acid, acid chloride, or acid anhydride.
  • the 5-hydroxy compounds are precursors of both the 5-aryloxy and 5-heteroaryloxy via nucleophilic aromatic substitution at electron deficient aromatic rings (e.g., 4-fluorobenzonitrile and 2,4-dichloropyrimidine).
  • Such chemistry is well known to those skilled in the art of organic synthesis.
  • Non-aromatic heterocyclyloxy derivatives can also be prepared from the 5-hydroxy compounds via Mitsunobu chemistry, in which a trialkyl- or triarylphosphine and diethyl azodicarboxylate are typically used. See Hughes, Org. React. (N.Y.) 42: 335 (1992) and Hughes, Org. Prep. Proced. Int. 28: 127 (1996).
  • various N-substituted-4-hydroxypiperidines can be coupled with the 5- hydroxypyridine compounds to give compounds bearing N-substituted piperidinyloxy substituents in the 5 position of the pyridine ring.
  • 5-Cyano-substituted analogs of the aforementioned compounds can be hydrolyzed to afford the corresponding 5-carboxamido-substituted compounds. Further hydrolysis results in formation of the corresponding 5-carboxylic acid- substituted analogs. Reduction of the 5-cyano-substituted analogs with lithium
  • the 5-hydroxymethyl-substituted analogs can be reacted with tosyl chloride to provide the corresponding 5-tosyloxymethyl analogs.
  • the 5-carboxylic acid-substituted analogs can also be converted to the corresponding 5-alkylaminoacyl analogs by reaction with an appropriate alkylamine and thionyl chloride. Certain of these amides are known to readily undergo nucleophilic acyl substitution to produce ketones.
  • Weinreb amides N-methoxy-N-methylamides
  • aryllithium reagents for example, see Selnick et al., Tet. Lett. 34: 2043 (1993).
  • 5-Tosyloxymethyl-substituted analogs of the aforementioned compounds can be converted to the corresponding 5 -methyl-substituted compounds by reduction with lithium aluminum hydride.
  • 5-Tosyloxymethyl-substituted analogs of the aforementioned compounds can also be used to produce 5-alkyl-substituted compounds via reaction with an alkyllithium.
  • 5-Hydroxy-substituted analogs of the aforementioned compounds can be used to prepare 5-N-alkylcarbamoyloxy- substituted compounds by reaction with N-alkylisocyanates.
  • 5-Amino-substituted analogs of the aforementioned compounds can be used to prepare 5-N- alkoxycarboxamido-substituted compounds by reaction with alkyl chloroformate esters, using techniques known to those skilled in the art of organic synthesis.
  • Chemistries analogous to those described hereinbefore for the preparation of 5-substituted (pyridine) analogs of diazabicyclic compounds can be devised for the synthesis of analogs bearing substituents in the 2, 4, and 6 positions of the pyridine ring.
  • a number of 2-, 4-, and 6-aminopyridyl diazabicyclic compounds can be converted to the corresponding diazonium salt intermediates, which can be transformed to a variety of compounds with substituents at the 2, 4, and 6 positions of the pyridine ring as was described for the 5-substituted analogs above.
  • the requisite 2-, 4-, and 6-aminopyridyl diazabicycles are available via the Chichibabin reaction of unsubstituted pyridyl diazabicycles (e.g., 5-benzyl-2-(3-pyridyl)-2,5- diazabicyclo[2.2.1]heptane, described previously). Similar reactions are described in Chemistry of Heterocyclic Compounds, Volume 14, part 3, pp.3-5 (Interscience Publishers, 1962) and by Lahti et al., J Med. Chem. 42: 2227 (1999). After the desired pyridine ring functional group manipulation has been accomplished, the benzyl protecting group can be removed from the diazabicycle using hydrogenation conditions.
  • 3,5-dibromopyridine can be converted into the corresponding 3-bromo-5-alkoxy- and 3-bromo-5-aryloxypyridines by the action of sodium alkoxides or sodium aryloxides.
  • Procedures such as those described by Comins et al., J Org. Chem. 55: 69 (1990) and Hertog et al., Recueil Trav. Chim. Pays-Bas 74: 1171 (1955) are used.
  • Compounds of the present invention can also be produced using 5- bromonicotinic acid as a precursor.
  • the acid can be converted to the acyl chloride (using thionyl chloride) and subsequently used in Friedel-Crafts-type acylations, producing 3-bromo-5-(arylcarbonyl)pyridines, which then serve as substrates for the palladium-catalyzed coupling reaction described earlier. See, for example, Villani and King, Org. Syn. Coll. Vol. 4: 88 (1963).
  • the present invention also relates to the use of other diazabicyclic systems in palladium-catalyzed coupling reactions with aryl halides.
  • the procedures described by Old et al., J Am. Chem. Soc. 120:9722 (1998) and Hartwig et al., J. Org. Chem. 64:5575 (1999) are typical of the conditions used for the coupling.
  • coupling of 3-bromopyridine with 6-carboethoxy-3,6-diazabicyclo[3.2.2]nonane under palladium catalysis will provide 3-(3-pyridyl)-6-carboethoxy-3,6- diazabicyclo[3.2.2]nonane.
  • 6-Carboethoxy-3,6- ⁇ diazabicyclo[3.2.2]nonane can be produced from 3-benzyl-6-carboethoxy-3,6- diazabicyclo[3.2.2]nonane by hydrogenation in the presence of palladium on carbon.
  • the synthesis of the requisite 3-benzyl-6-carboethoxy-3,6-diazabicyclo[3.2.2]nonane is described by Fray et al., J Org. Chem.
  • the 3,6-diazabicyclo[3.2.2]nonane ring system can also be coupled to aryl halides via the 6-aza position, producing 6-aryl-3,6-diazabicyclo[3.2.2]nonanes, which are isomeric to the 3-aryl-3,6-diazabicyclo[3.2.2]nonanes described previously.
  • the aforementioned 3-benzyl-6-carboethoxy-3,6-diazabicyclo[3.2.2]nonane can be hydrolyzed to 3-benzyl-3,6-diazabicyclo[3.2.2]nonane, which can subsequently be coupled to an aryl halide in a palladium-catalyzed reaction.
  • the 6-aryl-3-benzyl-3,6- diazabicyclo[3.2.2]nonane product can then be hydrogenated to give a 6-aryl-3,6- diazabicyclo[3.2.2]nonane.
  • diazabicyclic analog which can be incorporated into compounds of the present invention, is 3,6-diazabicyclo[3.2.1]octane.
  • 3,6-diazabicyclo[3.2.1]octane is 3,6-diazabicyclo[3.2.1]octane.
  • the synthesis of both 3-methyl-3,6-diazabicyclo[3.2.1]octane and 6-methyl-3,6- diazabicyclo[3.2.1]octane is described in European Patent Application No. 88305925.5, filed June 28, 1988 (Publication No. 0297858A2).
  • Either of these amines can be coupled with 3-bromopyridine, in a palladium-catalyzed process, to give isomeric products 3-methyl-6-(3-pyridyl)-3,6-diazabicyclo[3.2.1]octane and 6- methyl-3-(3-pyridyl)-3,6-diazabicyclo[3.2.1]octane.
  • the use of other appropriately substituted aryl halides in the coupling reaction will lead to other N-aryl 3,6- diazabicyclo[3.2. l]octane products.
  • Yet another diazabicycle that is illustrative of the present invention is the 3,7- diazabicyclo[3.3.1]nonane ring system.
  • 3,7-dibenzyl-3,7- diazabicyclo[3.3.1]nonan-9-one which is readily prepared by a double Mannich reaction of N-benzyl-4-piperidone with formaldehyde and benzylamine (see Garrison et al., J. Org. Chem. 58: 7670 (1993)), can be converted into 3,7-dibenzyl-3,7- diazabicyclo[3.3.1]nonane by either of several deoxygenation reactions. For instance, a Wolff-Kishner reduction, using procedures similar to those described by Berlin et al., Org. Prep, and Proc. Int.
  • the present invention relates to a method for providing prevention of a condition or disorder to a subject susceptible to such a condition or disorder, and for providing treatment to a subject suffering therefrom.
  • the method comprises administering to a patient an amount of a compound effective for providing some degree of prevention of the progression of a CNS disorder (i.e., provide protective effects), amelioration of the symptoms of a CNS disorder, and amelioration of the recurrence of a CNS disorder.
  • the method involves administering an effective amount of a compound selected from the general formulae, which are set forth hereinbefore.
  • the present invention relates to a pharmaceutical composition incorporating a compound selected from the general formulae, which are set forth hereinbefore.
  • Optically active compounds can be employed as racemic mixtures or as pure enantiomers.
  • the compounds can be employed in a free base form or in a salt form (e.g., as pharmaceutically acceptable salts).
  • suitable pharmaceutically acceptable salts include inorganic acid addition salts such as hydrochloride, hydrobromide, sulfate, phosphate, and nitrate; organic acid addition salts such as acetate, galactarate, propionate, succinate, lactate, glycolate, malate, tartrate, citrate, maleate, fumarate, methanesulfonate, p-toluenesulfonate, and ascorbate; salts with an acidic amino acid such as aspartate and glutamate; alkali metal salts such as sodium and potassium; alkaline earth metal salts such as magnesium and calcium; ammonium salt; organic basic salts such as trimethylamine, triethylamine, pyridine, picoline, dicyclohexylamine,
  • the salts may be in some cases hydrates or ethanol solvates.
  • Representative salts are provided as described in U.S. Patent Nos. 5,597,919 to Dull et al., 5,616,716 to Dull et al. and 5,663,356 to Ruecroft et al., the disclosures of which are incorporated herein by reference in their entirety.
  • Compounds of the present invention are useful for treating those types of conditions and disorders for which other types of nicotinic compounds have been proposed as therapeutics. See, for example, Williams et al., Drug News Perspec 7(4):205 (1994), Arneric et al., CNS Drug Rev. 1(1).T (1995), Arneric et al., Exp. Opin. Invest. Drugs 5(1):79 (1996), Bencherif et al., J Pharmacol. Exp. Ther. 279:1413 (1996), Lippiello et al., J Pharmacol. Exp. Ther. 279:1422 (1996), Damaj et al, J Pharmacol. Exp. Ther.
  • Compounds of the present invention can be used as analgesics, to treat ulcerative colitis, inflammatory and autoimmune diseases (e.g., arthritis, cholangitis, stomatitis, pouchitis, viral pneumonitis), to treat a variety of neurodegenerative diseases, and to treat convulsions such as those that are symptomatic of epilepsy.
  • inflammatory and autoimmune diseases e.g., arthritis, cholangitis, stomatitis, pouchitis, viral pneumonitis
  • convulsions such as those that are symptomatic of epilepsy.
  • CNS disorders which can be treated in accordance with the present invention include pre-senile dementia (early onset Alzheimer's disease), senile dementia (dementia of the Alzheimer's type), HIV- dementia, multiple cerebral infarcts, Parkinsonism including Parkinson's disease, Pick's disease, Huntington's chorea, tardive dyskinesia, hyperkinesia, mania, attention deficit disorder, anxiety, depression, mild cognitive impairment, dyslexia, schizophrenia and Tourette's syndrome.
  • Compounds of the present invention also can be used to treat conditions such as syphillis and Creutzfeld- Jakob disease.
  • the compounds of the present invention also can be appropriately synthesized and used as or within pharmaceutical compositions that are used as diagnostic probes.
  • the pharmaceutical composition also can include various other components as additives or adjuncts.
  • exemplary pharmaceutically acceptable components or adjuncts which are employed in relevant circumstances include antioxidants, free- radical scavenging agents, peptides, growth factors, antibiotics, bacteriostatic agents, immunosuppressives, anticoagulants, buffering agents, anti-inflammatory agents, antipyretics, time-release binders, anaesthetics, steroids, vitamins, minerals and corticosteroids.
  • Such components can provide additional therapeutic benefit, act to affect the therapeutic action of the pharmaceutical composition, or act towards preventing any potential side effects which may be imposed as a result of administration of the pharmaceutical composition.
  • a compound of the present invention can be employed as part of a pharmaceutical composition with other compounds intended to prevent or treat a particular disorder.
  • the manner in which the compounds are administered can vary.
  • the compounds can be administered by inhalation (e.g., in the form of an aerosol either nasally or using delivery articles of the type set forth in U.S. Patent No. 4,922,901 to Brooks et al., the disclosure of which is incorporated herein in its entirety); topically (e.g., in lotion form); orally (e.g., in liquid form within a solvent such as an aqueous or non-aqueous liquid, or within a solid carrier); intravenously (e.g., within a dextrose or saline solution); as an infusion or injection (e.g., as a suspension or as an emulsion in a pharmaceutically acceptable liquid or mixture of liquids); intrathecally; intracerebroventricularly; or transdermally (e.g., using a transdermal patch).
  • inhalation e.g., in the form of an aerosol either nasally or using delivery articles of the type set forth in U.S
  • each compound in the form of a pharmaceutical composition or formulation for efficient and effective administration.
  • exemplary methods for administering such compounds will be apparent to the skilled artisan.
  • the compounds can be administered in the form of a tablet, a hard gelatin capsule or as a time-release capsule.
  • the compounds can be delivered transdermally using the types of patch technologies available from Novartis and Alza Corporation.
  • the administration of the pharmaceutical compositions of the present invention can be intermittent or at a gradual, continuous, constant or controlled rate to a warm-blooded animal (e.g., a mammal such as a mouse, rat, cat, rabbit, dog, pig, cow, or monkey), but advantageously is administered preferably to a human being.
  • a warm-blooded animal e.g., a mammal such as a mouse, rat, cat, rabbit, dog, pig, cow, or monkey
  • the time of day and the number of times per day that the pharmaceutical formulation is administered can vary.
  • Preferable administration is such that the active ingredients of the pharmaceutical formulation interact with receptor sites within the body of the subject that affect the functioning of the CNS. More specifically, in treating a CNS disorder, preferable administration is designed to optimize the effect upon those relevant receptor subtypes that have an effect upon the functioning of the CNS, while minimizing the effects upon muscle- type receptor subtypes.
  • Other suitable methods for administering the compounds of the present invention are described in U.
  • an effective amount of compound is an amount sufficient to pass across the blood-brain barrier of the subject, to bind to relevant receptor sites in the brain of the subject and to activate relevant nicotinic receptor subtypes (e.g., provide neurotransmitter secretion, thus resulting in effective prevention or treatment of the disorder).
  • an effective amount of compound is an amount sufficient to pass across the blood-brain barrier of the subject, to bind to relevant receptor sites in the brain of the subject and to activate relevant nicotinic receptor subtypes (e.g., provide neurotransmitter secretion, thus resulting in effective prevention or treatment of the disorder).
  • Prevention of the disorder is manifested by delaying the onset of the symptoms of the disorder. Treatment of the disorder is manifested by a decrease in the symptoms associated with the disorder or an amelioration of the recurrence of the symptoms of the disorder.
  • the effective dose can vary, depending upon factors such as the condition of the patient, the severity of the symptoms of the disorder, and the manner in which the pharmaceutical composition is administered.
  • the effective dose of typical compounds generally requires administering the compound in an amount sufficient to activate relevant receptors to effect neurotransmitter (e.g., dopamine) release, but the amount should be insufficient to induce effects on skeletal muscles and ganglia to any significant degree.
  • the effective dose of compounds will of course differ from patient to patient, but in general includes amounts starting where CNS effects or other desired therapeutic effects occur but below the amount where muscular effects are observed.
  • the compounds useful according to the method of the present invention have the ability to pass across the blood-brain barrier of the patient. As such, these compounds have the ability to enter the central nervous system of the patient.
  • the log P values of typical compounds, which are useful in carrying out the present invention are generally greater than about -0.5, often are greater than about 0, and frequently are greater than about 0.5.
  • the log P values of such typical compounds generally are less than about 3, often are less than about 2, and frequently are less than about 1.
  • Log P values provide a measure of the ability of a compound to pass across a diffusion barrier, such as a biological membrane, including the blood brain barrier. See, for example, Hansch et al., J Med. Chem.ll (1968).
  • the compounds useful according to the method of the present invention have the ability to bind to, and in most circumstances, cause activation of, nicotinic dopaminergic receptors of the brain of the patient. As such, these compounds have the ability to express nicotinic pharmacology and, in particular, to act as nicotinic agonists.
  • the receptor binding constants of typical compounds useful in carrying out the present invention generally exceed about 0.1 nM, often exceed about 1 nM, and frequently exceed about 10 nM.
  • the receptor binding constants of certain compounds are less than about 100 ⁇ M, often are less than about 10 ⁇ M and frequently are less than about 5 ⁇ M; and of preferred compounds generally are less than about 2.5 ⁇ M, sometimes are less than about 1 ⁇ M, and can be less than about 100 nM.
  • Receptor binding constants provide a measure of the ability of the compound to bind to half of the relevant receptor sites of certain brain cells of the patient. See, for example, Cheng et al, Biochem. Pharmacol 22:3099 (1973).
  • the compounds useful according to the method of the present invention have the ability to demonstrate a nicotinic function by effectively activating neurotransmitter secretion from nerve ending preparations (i.e., synaptosomes). As such, these compounds have the ability to activate relevant neurons to release or secrete acetylcholine, dopamine, and other neurotransmitters.
  • typical compounds useful in carrying out the present invention provide for the activation of dopamine secretion in amounts of at least one third, typically at least about 10 times less, frequently at least about 100 times less, and sometimes at least about 1,000 times less than those required for activation of muscle-type nicotinic receptors.
  • Certain compounds of the present invention can provide secretion of dopamine in an amount which is comparable to that elicited by an equal molar amount of (S)-(-)-nicotine.
  • the compounds of the present invention when employed in effective amounts in accordance with the method of the present invention, are selective to certain relevant nicotinic receptors, but do not cause significant activation of receptors associated with undesirable side effects at concentrations at least greater than those required for activation of dopamine release.
  • a particular dose of compound resulting in prevention and/or treatment of a CNS disorder is essentially ineffective in eliciting activation of certain ganglionic-type nicotinic receptors at concentration higher than 5 times, preferably higher than 100 times, and more preferably higher than 1,000 times than those required for activation of dopamine release.
  • Compounds of the present invention when employed in effective amounts in accordance with the method of the present invention, are effective towards providing some degree of prevention of the progression of CNS disorders, amelioration of the symptoms of CNS disorders, and amelioration to some degree of the recurrence of CNS disorders.
  • effective amounts of those compounds are not sufficient to elicit any appreciable side effects, as demonstrated by increased effects relating to skeletal muscle.
  • administration of certain compounds of the present invention provides a therapeutic window in which treatment of certain CNS disorders is provided and certain side effects are avoided. That is, an effective dose of a compound of the present invention is sufficient to provide the desired effects upon the CNS but is insufficient (i.e., is not at a high enough level) to provide undesirable side effects.
  • effective administration of a compound of the present invention resulting in treatment of CNS disorders occurs upon administration of less than 1/5, and often less than 1/10, that amount sufficient to cause certain side effects to any significant degree.
  • the pharmaceutical compositions of the present invention can be employed to prevent or treat certain other conditions, diseases and disorders.
  • diseases and disorders include inflammatory bowel disease, pouchitis, acute cholangitis, aphthous stomatitis, arthritis (e.g., rheumatoid arthritis and osteoarthritis), neurodegenerative diseases, cachexia secondary to infection (e.g., as occurs in AIDS, AIDS-related complex and neoplasia), as well as those indications set forth in PCT WO 98/25619.
  • the pharmaceutical compositions of the present invention can be employed in order to ameliorate many of the symptoms associated with those conditions, diseases and disorders.
  • compositions of the present invention can be used in treating genetic diseases and disorders, in treating autoimmune disorders such as lupus, as anti-infectious agents (e.g., for treating bacterial, fungal and viral infections, as well as the effects, such as sepsis, of other types of toxins), as anti-inflammatory agents (e.g., for treating acute cholangitis, aphthous stomatitis, asthma, and ulcerative colitis), and as inhibitors of cytokine release (e.g., as is desirable in the treatment of cachexia, inflammation, neurodegenerative diseases, viral infection, and neoplasia).
  • autoimmune disorders such as lupus
  • anti-infectious agents e.g., for treating bacterial, fungal and viral infections, as well as the effects, such as sepsis, of other types of toxins
  • anti-inflammatory agents e.g., for treating acute cholangitis, aphthous stomatitis, asthma, and ulcerative colitis
  • the compounds of the present invention can also be used as adjunct therapy in combination with existing therapies in the management of the aforementioned types of diseases and disorders.
  • preferable administration is such that the active ingredients of the pharmaceutical formulation act to optimize effects upon abnormal cytokine production, while minimizing effects upon receptor subtypes such as those that are associated with muscle and ganglia.
  • Preferable administration is such that active ingredients interact with regions where cytokine production is affected or occurs.
  • compounds of the present invention are very potent (i.e., affect cytokine production and/or secretion at very low concentrations) and are very efficacious (i.e., significantly inhibit cytokine production and/or secretion to a relatively high degree).
  • effective doses are at very low concentrations, where maximal effects are observed to occur. Concentrations, determined as the amount of compound per volume of relevant tissue, typically provide a measure of the degree to which that compound affects cytokine production. Typically, the effective dose of such compounds generally requires administering the compound in an amount of less than 5 mg/kg of patient weight. Often, the compounds of the present invention are administered in an amount from less than about 1 mg/kg patent weight and usually less than about 100 ⁇ g/kg of patient weight, but frequently between about 10 ⁇ g to less than 100 ⁇ g/kg of patient weight.
  • the effective dose is less than 5 mg/kg of patient weight; often such compounds are administered in an amount from 50 ⁇ g to less than 5 mg/kg of patient weight.
  • the foregoing effective doses typically represent that amount administered as a single dose, or as one or more doses administered over a 24-hour period.
  • the effective dose of typical compounds generally requires administering the compound in an amount of at least about 1, often at least about 10, and frequently at least about 25 ⁇ g/ 24 hr/ patient.
  • the effective dose of typical compounds requires administering the compound which generally does not exceed about 500, often does not exceed about 400, and frequently does not exceed about 300 ⁇ g/ 24 hr/ patient.
  • administration of the effective dose is such that the concentration of the compound within the plasma of the patient normally does not exceed 500 pg/mL, often does not exceed 300 pg/mL, and frequently does not exceed 100 pg/mL.
  • compounds of the present invention are dose dependent, and, as such, cause inhibition of cytokine production and/or secretion when employed at low concentrations but do not exhibit those inhibiting effects at higher concentrations.
  • Compounds of the present invention exhibit inhibitory effects upon cytokine production and/or secretion when employed in amounts less than those amounts necessary to elicit activation of relevant nicotinic receptor subtypes to any significant degree.
  • Binding of the compounds to relevant receptor sites was determined in accordance with the techniques described in U.S. Patent No. 5,597,919 to Dull et al. Inhibition constants (Kj values), reported in nM, were calculated from the IC 50 values using the method of Cheng et al., Biochem. Pharmacol 22:3099 (1973).
  • Kj values Inhibition constants
  • Sample No. 1 is (lS,4S)-2-(5-(4-methoxyphenoxy)-3-pyridy ⁇ )-2,5- diazabicyclo[2.2.1]heptane hemigalactarate, which was prepared in accordance with the following techniques:
  • the reaction mixture was poured into saturated aqueous sodium chloride solution (20 mL) and extracted with diethyl ether (3 x 30 mL). The combined diethyl ether extracts were washed with saturated aqueous sodium chloride solution (20 mL), dried (Na 2 SO 4 ), filtered and concentrated to a brown oil (0.37 g). The material was used without further purification.
  • the aqueous portion was adjusted to pH 11 using 10% NaOH, followed by extraction with diethyl ether (3 x 25 mL). The combined diethyl ether extracts were dried (Na SO 4 ), filtered and concentrated under vacuum to give a yellow oil (0.26 g). The material was used without further purification.
  • Sample No. 1 exhibits a Kj of 13 nM.
  • the low binding constant indicates that the compound exhibits good high-affinity binding to certain CNS nicotinic receptors.
  • Sample No. 2 is (lS,4S)-2-(5-(3-methoxyphenoxy)-3-pyridyl)-2,5- diazabicyclo[2.2.1]heptane hemigalactarate, which was prepared in accordance with the following techniques:
  • 3-bromo-5-(3-methoxyphenoxy)pyridine was prepared using 3-methoxyphenol (2.79 g, 0.023 mole), 75% sodium hydride suspension in oil (0.72 g, 0.023 mol) in dimethylformamide (20 mL) and 3,5- dibromopyridine (3.55 g, 0.015 mol).
  • the reaction was worked up using water (50 mL), 5 N NaOH solution (5 mL), and diethyl ether (3 x 50 mL), and a yellow oil (4.6 g) was obtained as crude product.
  • This oil was purified by column chromatography on silica gel, eluting with cyclohexane-ethyl acetate (92.5 : 7.5, v/v). Selected fractions containing the product were concentrated via rotary evaporation to give 2.3 g (55 %) of a yellow oil.
  • the aqueous portion was adjusted to pH 11 using 10 % NaOH, followed by extraction with diethyl ether (3 x 25 mL).
  • the combined diethyl ether extracts were dried (Na 2 SO 4 ), filtered, and concentrated under vacuum to give a colorless oil (0.41 g, 82%).
  • Sample No. 2 exhibits a Ki of 4 nM.
  • the low binding constant indicates that the compound exhibits good high-affinity binding to certain CNS nicotinic receptors.
  • Sample No. 3 is (lS,4S)-2-(5-(4-fluorophenoxy)-3-pyridyl)-2,5- diazabicyclo[2.2.1]heptane dihydrochloride, which was prepared in accordance with the following techniques: 3-Bromo-5-(4-fluorophenoxy)pyridine
  • the reaction mixture was cooled to room temperature and diluted with water (150 mL) and then extracted with diethyl ether (2 x 100 mL). The combined diethyl ether extracts were dried (MgSO 4 ), filtered and concentrated by rotary evaporation. The residue was purified by flash chromatography on silica gel, using a gradient of 33% to 67% ethyl acetate :hexane as eluent, to yield 1.8 g (90%) of a yellow oil.
  • Sample No. 3 exhibits a K, of 12 nM.
  • the low binding constant indicates that the compound exhibits good high-affinity binding to certain CNS nicotinic receptors. .
  • Sample No. 4 is (lS,4S)-2-(5-(3-thienyl)-3-pyridyl)-2,5- diazabicyclo[2.2.1]heptane, which was prepared in accordance with the following techniques:
  • Sample No. 4 exhibits a Kj of 670 nM.
  • the low binding constant indicates that the compound exhibits good high-affinity binding to certain CNS nicotinic receptors.
  • Sample No. 5 is (lS,4S)-2-(5-benzoyl-3-pyridyl)-2,5- diazabicyclo[2.2.1]heptane dihydrochloride, which was prepared in accordance with the following techniques:
  • the aqueous layer containing an emulsion, was treated with 50% aqueous NaOH until the aluminum salts redissolved. After cooling, the product was extracted with chloroform (2 x 200 mL). The combined chloroform layers were dried (Na SO 4 ), filtered and concentrated. The residue was purified by flash chromatography on silica gel, using ethyl acetate:hexane (1 :5) as eluent, to yield 2.5 g (9.5%) of off-white crystals; m.p. 66-68°C.
  • the reaction mixture was cooled to room temperature and diluted with water (200 mL) and then extracted with diethyl ether (100 mL).
  • the diethyl ether extract was dried (MgSO ), filtered and concentrated by rotary evaporation.
  • the residue was purified by flash chromatography on silica gel, using a gradient of 50% to 80% ethyl acetate :hexane as eluent, to yield 0.364 g (48%) of a yellow oil.
  • Sample No. 5 exhibits a Kj of 122 nM.
  • the low binding constant indicates that the compound exhibits good high-affinity binding to certain CNS nicotinic receptors.

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Abstract

La présente invention concerne des composés diazabicycliques, de préférence, des composés diazabicycliques de N-aryle. Des composés particulièrement intéressants sont les composés de 2-pyridyle diazabicyclique comme (1S,4S)-2-(5-(3-méthoxyphénoxy)-3-pyridyl)-2,5-diazabicyclo[2.2.1]heptane. D'autres composés représentant des exemples de la présente invention comprennent: (1S,4S)-2-(5-(4-méthoxyphénoxy)-3-pyridyl)-2,5-diazabicyclo[2.2.1]heptane, (1S,4S)-2-(5-(3,4-diméthoxyphénoxy)-3-pyridyl)-2,5-diazabicyclo[2.2.1]heptane, (1S,4S)-2-(5-(4-fluorophénoxy)-3-pyridyl)-2,5-diazabicyclo[2.2.1]heptane, et (1S,4S)-2-(5-benzoyl-3-pyridyl)-2,5-diazabicyclo[2.2.1]heptane. La présente invention concerne également des dérivés des composés de la présente invention constituant des promédicaments.
PCT/US2001/016941 2000-05-25 2001-05-24 Heteroaryldiazabicycloalkanes comme ligands du recepteur cholinergique nicotinique WO2001090109A1 (fr)

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AU2001274952A AU2001274952A1 (en) 2000-05-25 2001-05-24 Heteroaryldiazabicycloalkanes as nicotinic cholinergic receptor ligands
BR0110956-1A BR0110956A (pt) 2000-05-25 2001-05-24 Heteroarildiazabicicloalcanos como ligantes do receptor colinérgico nicotìnico
DK01941614T DK1289996T3 (da) 2001-05-24 2001-05-24 Heteroaryldiazabicycloalkaner som nicotiniske cholinergiske receptorligander
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JP2003534344A (ja) 2003-11-18
US6852721B2 (en) 2005-02-08
MXPA02011261A (es) 2003-03-10
CN1195756C (zh) 2005-04-06
WO2001090109A9 (fr) 2003-03-27
USRE41439E1 (en) 2010-07-13
DE60109924D1 (de) 2005-05-12
PT1289996E (pt) 2005-07-29
BR0110956A (pt) 2003-06-10
DE60109924T2 (de) 2006-02-09
CA2409644A1 (fr) 2001-11-29
ATE292636T1 (de) 2005-04-15
ES2242749T3 (es) 2005-11-16
CN1436191A (zh) 2003-08-13
EP1289996A1 (fr) 2003-03-12
AU2001274952A1 (en) 2001-12-03
KR20030004425A (ko) 2003-01-14
US20020013309A1 (en) 2002-01-31

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